FDA Drug Recalls

Recalls / Class II

Class IID-1041-2016

Product

VERMOX Tablets 100 mg; 6-count box, UPC 7501109900619

Affected lot / code info
Lot # UPE187; Exp. 08/17

Why it was recalled

CGMP Deviations

Recalling firm

Firm
Profarma Distributors LLC
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
4751 Poth Rd, N/A, Columbus, Ohio 43213-1331

Distribution

Quantity
163 boxes (978 tablets)
Distribution pattern
Nationwide

Timeline

Recall initiated
2016-05-11
FDA classified
2016-06-17
Posted by FDA
2016-06-29
Terminated
2017-01-24
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-1041-2016. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.